Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 134675016 | Properdin deficiency disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 504630014 | Properdin deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 822407019 | Properdin deficiency disease (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Properdin deficiency disease | Pathological process | Abnormal immune process | true | Inferred relationship | Some | 2 | |
| Properdin deficiency disease | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
| Properdin deficiency disease | Is a | Alternative pathway deficiency | true | Inferred relationship | Some | ||
| Properdin deficiency disease | Finding site | Structure of immune system | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR